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510(k) Data Aggregation
(116 days)
VEA Align:
This cloud-based software is intended for orthopedic applications in both pediatric and adult populations.
2D X-ray images acquired in EOS imaging's imaging systems is the foundation and resource to display the interactive landmarks overlayed on the frontal and lateral mages. These landmarks are available for users to assess patient-specific global alignment.
For additional assessment, alignment parameters compared to published normative values may be available.
This product serves as a tool to aid in the analysis of spinal deformities and degenerative diseases, and lower limb alignment disorders and deformities through precise and length measurements. It is suitable for use with adult and pediatric patients aged 7 years and older.
Clinical judgment and experience are required to properly use the software.
spineEOS:
spineEOS is indicated for assisting healthcare professionals with preoperative planning of spine surgeries. The product provides access to EOS images with associated 3D datasets and measurements. spineEOS includes surgical planning tools that enable users to define a patient specific surgical strategy.
VEA Align is a software indicated for assisting healthcare professionals with global alignment assessment through clinical parameters computation. The product uses biplanar 2D X-ray images, exclusively generated by EOS imaging's EOS (K152788) and EOSedge (K202394) systems and generates an initial placement of the patient anatomic landmarks on the images using a machine learning-based algorithm. The user may adjust the landmarks to align with the patient's anatomy. Landmark locations require user validation. The clinical parameters communicated to the user are inferred from the landmarks and are recalculated as the user adjusts the landmarks. 3D datasets may be exported for use in spineEOS for surgical planning. The product is hosted on a cloud infrastructure and relies on VEA Portal for support capabilities, such as user access control and data access. 2D X-ray image transmissions from healthcare institutions to the cloud are managed by VEA Portal is a Class | 510(k)-exempt device (LMD).
spineEOS is a software indicated for assisting healthcare professionals with preoperative planning of spine surgeries. EOS images (generated from EOS imaging's acquisition system) and associated 3D datasets are used as inputs of the software. The product manages clinical measurements and allows user to access surgical planning tools to define a patient specific surgical strategy. The product is indicated for adolescent and adult patients.
The provided text describes the performance data for the VEA Align device, focusing on the standalone performance of its AI algorithm.
Here's the breakdown of the acceptance criteria and the study proving the device meets them:
1. A table of acceptance criteria and the reported device performance
Acceptance Criteria | Reported Device Performance |
---|---|
Spinal Landmark Accuracy: | |
Median error ≤ 3 mm (Euclidean distance) | Met acceptance criteria for algorithm performance (Direct comparison between skeletal landmark locations between the subject device and predicate VEA Align (K231917)). Also met for additional spinal landmarks when compared to predicate sterEOS Workstation (K172346). |
3rd Quartile ≤ 5 mm (Euclidean distance) | Met acceptance criteria for algorithm performance (Direct comparison between skeletal landmark locations between the subject device and predicate VEA Align (K231917)). Also met for additional spinal landmarks when compared to predicate sterEOS Workstation (K172346). |
Spinal Mesh Accuracy: | |
Median error ≤ 3 mm (Point to surface distance) | Met acceptance criteria (Direct comparison between the 3D thoraco-lumbar mesh from the subject device and the 3D thoraco-lumbar mesh from the predicate sterEOS Workstation (K172346)). |
3rd Quartile ≤ 5 mm (Point to surface distance) | Met acceptance criteria (Direct comparison between the 3D thoraco-lumbar mesh from the subject device and the 3D thoraco-lumbar mesh from the predicate sterEOS Workstation (K172346)). |
2. Sample size used for the test set and the data provenance
- Test set sample size: 538 patients.
- Data provenance: Not explicitly stated as country of origin, but the images were collected from EOS (K152788) and EOSedge (K202394) systems at a variety of sites. The subgroup analysis includes "US vs. OUS" (Outside US), implying international data. The data collection period was from 2007-2023. The study seems to be retrospective as it uses previously collected images.
3. Number of experts used to establish the ground truth for the test set and the qualifications of those experts
The document states that the ground truth for the test set was an "EOS 3DServices reconstruction (model) from sterEOS Workstation (K172346)". It does not explicitly state the number or qualifications of experts used to establish this ground truth for the test set. However, the nature of the sterEOS Workstation suggests that these 3D reconstructions are typically performed or validated by trained specialists.
4. Adjudication method (e.g., 2+1, 3+1, none) for the test set
The document does not specify an adjudication method for the test set ground truth. It relies on the "ground truth EOS 3DServices reconstruction (model) from sterEOS Workstation (K172346)."
5. If a multi-reader multi-case (MRMC) comparative effectiveness study was done, If so, what was the effect size of how much human readers improve with AI vs without AI assistance
No MRMC comparative effectiveness study was described where human readers' improvement with AI vs. without AI assistance was evaluated. The performance testing focused on the standalone performance of the AI algorithm. The VEA Align device involves a machine learning-based algorithm for initial landmark placement, but then explicitly states, "The user may adjust the landmarks to align with the patient's anatomy. Landmark locations require user validation." This implies a human-in-the-loop system, but the described performance study is primarily on the algorithm's initial accuracy, not human improvement.
6. If a standalone (i.e., algorithm only without human-in-the-loop performance) was done
Yes, a standalone performance test of the AI algorithm was done. The document explicitly states: "To assess the standalone performance of the Al algorithm of the VEA Align, the test was performed with..."
7. The type of ground truth used (expert consensus, pathology, outcomes data, etc.)
The ground truth used for the standalone algorithm performance was "a ground truth EOS 3DServices reconstruction (model) from sterEOS Workstation (K172346)". This suggests a reconstructed anatomical model derived from clinically used software, likely validated by trained operators or experts who generated that model previously.
8. The sample size for the training set
The AI algorithm was trained using 10,376 X-ray images and a total of 5,188 corresponding 3D reconstructions.
9. How the ground truth for the training set was established
The document states that the training data included "corresponding 3D reconstructions" presumably generated by sterEOS Workstation (K172346), similar to the test set ground truth. These 3D reconstructions would have been based on images from EOS systems and likely performed by trained personnel using the sterEOS Workstation. It's implied that these served as the ground truth for training the AI algorithm to generate its initial placements.
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